Evidence Details for PRTG
Basic Information Top
| Gene Symbol: | PRTG ( FLJ12795,FLJ13221,FLJ25756,IGDCC5 ) |
|---|---|
| Gene Full Name: | protogenin |
| Band: | 15q21.3 |
| Quick Links | Entrez ID:283659; OMIM: 613261; Uniprot ID:PRTG_HUMAN; ENSEMBL ID: ENSG00000166450; HGNC ID: 26373 |
| Relate to Another Database: | SFARIGene; denovo-db |
Sequences Top
>PRTG|283659|nucleotide
ATGGCGCCTCCTCTGCGACCCCTCGCCCGGCTGCGACCGCCGGGGATGCTGCTCCGCGCGCTCCTGCTCCTGCTGCTGCTCAGTCCTTTGCCAGGAGTGTGGTGC
TTTAGCGAACTGTCTTTTGTAAAAGAACCACAGGATGTAACTGTCACAAGAAAGGACCCAGTCGTTTTAGATTGCCAGGCTCACGGAGAAGTTCCTATTAAGGTC
ACATGGTTGAAAAATGGAGCAAAAATGTCTGAAAATAAACGGATCGAGGTTCTTTCTAACGGCTCTTTATACATCAGTGAGGTGGAAGGCAGGCGAGGAGAGCAG
TCCGATGAAGGATTTTATCAGTGCTTGGCAATGAACAAATATGGAGCCATTCTTAGTCAAAAAGCTCATCTTGCCTTATCAACTATTTCTGCATTTGAAGTCCAG
CCAATTTCCACTGAGGTCCACGAAGGTGGAGTTGCTCGATTTGCATGCAAGATTTCATCCCACCCTCCTGCAGTCATAACATGGGAGTTCAATCGGACAACTCTA
CCTATGACTATGGACAGGATAACTGCCCTACCAACAGGAGTATTGCAGATCTATGATGTCAGCCAAAGGGATTCTGGAAATTATCGTTGTATTGCTGCCACTGTA
GCCCACCGACGTAAAAGTATGGAGGCCTCGCTAACTGTGATTCCAGCTAAGGAGTCAAAATCCTTCCACACACCAACAATTATAGCAGGTCCACAGAACATAACA
ACATCTCTTCATCAGACTGTAGTTTTGGAATGCATGGCCACAGGAAATCCCAAACCAATCATTTCTTGGAGCCGCCTTGATCACAAATCCATTGATGTCTTTAAT
ACTCGGGTACTTGGAAATGGTAATCTCATGATATCTGATGTCAGGCTACAACATGCTGGAGTATATGTTTGTCGGGCCACTACCCCTGGCACACGCAACTTTACA
GTTGCTATGGCAACTTTAACTGTATTAGCTCCTCCTTCATTTGTTGAATGGCCAGAAAGTTTAACAAGGCCTCGAGCTGGCACTGCTCGATTTGTGTGTCAGGCA
GAAGGAATCCCCTCTCCCAAGATGTCATGGTTGAAAAATGGAAGGAAGATACATTCGAATGGTAGAATTAAAATGTACAACAGTAAATTGGTAATTAACCAGATT
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ATGGCGCCTCCTCTGCGACCCCTCGCCCGGCTGCGACCGCCGGGGATGCTGCTCCGCGCGCTCCTGCTCCTGCTGCTGCTCAGTCCTTTGCCAGGAGTGTGGTGC
TTTAGCGAACTGTCTTTTGTAAAAGAACCACAGGATGTAACTGTCACAAGAAAGGACCCAGTCGTTTTAGATTGCCAGGCTCACGGAGAAGTTCCTATTAAGGTC
ACATGGTTGAAAAATGGAGCAAAAATGTCTGAAAATAAACGGATCGAGGTTCTTTCTAACGGCTCTTTATACATCAGTGAGGTGGAAGGCAGGCGAGGAGAGCAG
TCCGATGAAGGATTTTATCAGTGCTTGGCAATGAACAAATATGGAGCCATTCTTAGTCAAAAAGCTCATCTTGCCTTATCAACTATTTCTGCATTTGAAGTCCAG
CCAATTTCCACTGAGGTCCACGAAGGTGGAGTTGCTCGATTTGCATGCAAGATTTCATCCCACCCTCCTGCAGTCATAACATGGGAGTTCAATCGGACAACTCTA
CCTATGACTATGGACAGGATAACTGCCCTACCAACAGGAGTATTGCAGATCTATGATGTCAGCCAAAGGGATTCTGGAAATTATCGTTGTATTGCTGCCACTGTA
GCCCACCGACGTAAAAGTATGGAGGCCTCGCTAACTGTGATTCCAGCTAAGGAGTCAAAATCCTTCCACACACCAACAATTATAGCAGGTCCACAGAACATAACA
ACATCTCTTCATCAGACTGTAGTTTTGGAATGCATGGCCACAGGAAATCCCAAACCAATCATTTCTTGGAGCCGCCTTGATCACAAATCCATTGATGTCTTTAAT
ACTCGGGTACTTGGAAATGGTAATCTCATGATATCTGATGTCAGGCTACAACATGCTGGAGTATATGTTTGTCGGGCCACTACCCCTGGCACACGCAACTTTACA
GTTGCTATGGCAACTTTAACTGTATTAGCTCCTCCTTCATTTGTTGAATGGCCAGAAAGTTTAACAAGGCCTCGAGCTGGCACTGCTCGATTTGTGTGTCAGGCA
GAAGGAATCCCCTCTCCCAAGATGTCATGGTTGAAAAATGGAAGGAAGATACATTCGAATGGTAGAATTAAAATGTACAACAGTAAATTGGTAATTAACCAGATT
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>PRTG|283659|protein
MAPPLRPLARLRPPGMLLRALLLLLLLSPLPGVWCFSELSFVKEPQDVTVTRKDPVVLDCQAHGEVPIKVTWLKNGAKMSENKRIEVLSNGSLYISEVEGRRGEQ
SDEGFYQCLAMNKYGAILSQKAHLALSTISAFEVQPISTEVHEGGVARFACKISSHPPAVITWEFNRTTLPMTMDRITALPTGVLQIYDVSQRDSGNYRCIAATV
AHRRKSMEASLTVIPAKESKSFHTPTIIAGPQNITTSLHQTVVLECMATGNPKPIISWSRLDHKSIDVFNTRVLGNGNLMISDVRLQHAGVYVCRATTPGTRNFT
VAMATLTVLAPPSFVEWPESLTRPRAGTARFVCQAEGIPSPKMSWLKNGRKIHSNGRIKMYNSKLVINQIIPEDDAIYQCMAENSQGSILSRARLTVVMSEDRPS
APYNVHAETMSSSAILLAWERPLYNSDKVIAYSVHYMKAEGLNNEEYQVVIGNDTTHYIIDDLEPASNYTFYIVAYMPMGASQMSDHVTQNTLEDVPLRPPEISL
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MAPPLRPLARLRPPGMLLRALLLLLLLSPLPGVWCFSELSFVKEPQDVTVTRKDPVVLDCQAHGEVPIKVTWLKNGAKMSENKRIEVLSNGSLYISEVEGRRGEQ
SDEGFYQCLAMNKYGAILSQKAHLALSTISAFEVQPISTEVHEGGVARFACKISSHPPAVITWEFNRTTLPMTMDRITALPTGVLQIYDVSQRDSGNYRCIAATV
AHRRKSMEASLTVIPAKESKSFHTPTIIAGPQNITTSLHQTVVLECMATGNPKPIISWSRLDHKSIDVFNTRVLGNGNLMISDVRLQHAGVYVCRATTPGTRNFT
VAMATLTVLAPPSFVEWPESLTRPRAGTARFVCQAEGIPSPKMSWLKNGRKIHSNGRIKMYNSKLVINQIIPEDDAIYQCMAENSQGSILSRARLTVVMSEDRPS
APYNVHAETMSSSAILLAWERPLYNSDKVIAYSVHYMKAEGLNNEEYQVVIGNDTTHYIIDDLEPASNYTFYIVAYMPMGASQMSDHVTQNTLEDVPLRPPEISL
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Evidence summary Top
Click the link of the category-specific score to view different category of evidences. The categories without any evidences are hidden by default.
| Evidences | Syndromic Gene | GWAS | CNV | Linkage | Association | Expression | NGS de novo | NGS Mosaic | NGS Other | Low-Scale Gene Studies | Total |
|---|---|---|---|---|---|---|---|---|---|---|---|
| Score (No. of Studies) | No | 0 (0) | 1 (2) | 1 (2) | 0 (0) | 0 (0) | 0 (0) | 0 (0) | 0 (0) | 0 (0) | 4 (4) |
Syndromic Autism Gene Top
Genome-Wide Association Studies(By Ethnic Group) Top
CNV Studies Top
| Reference | Source | Method | ADI-R | ADOS | Diagnosis | Family | Individual | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Total | Simplex | Multiplex | Control | Affected | Control | Total | ||||||
| Szatmari, 2007 | Europe, North America | SNP microarray | ![]() | ![]() | ASD | 1491 | - | - | - | - | - | 0 |
| Berkel, 2010 | Canada | SNP microarray | ![]() | ![]() | ASD | - | - | - | - | 396 | 5023 | 5419 |
Linkage Studies Top
| Reference | Source | Method | ADI-R | ADOS | Diagnosis | Family | Individual | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Total | Simplex | Multiplex | Control | Affected | Control | Total | ||||||
| Lauritsen, 2006 | Faroe Islands | microsatellite-based genomic screen | ![]() | ![]() | autism | - | - | - | - | 12 | 44 | 56 |
| Allen-Brady, 2010 | USA | SNP-based genomic screen | ![]() | ![]() | ASD | 40 | - | 40 | - | 192 | 461 | 653 |
Low Scale Association Studies (by Ethnic Group) Top
Large Scale Expression Studies Top
NGS de novo Mutation Studies Top
NGS Mosaic SNV Studies Top
NGS Other Studies Top
Low Scale Gene Studies Top
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